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venous thromboembolism
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factor VIII
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Rezende, S.M.
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Rosendaal, F.R.
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Lijfering, W.M.
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Cannegieter, S.C.
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Venous thromboembolism prophylaxis in foot and ankle surgery
Cardiovascular risk scores among asymptomatic adults with haemophilia
Time between inhibitor detection and start of immune tolerance induction: Association with outcome in the BrazIT study
Recurrence after stopping anticoagulants in women with combined oral contraceptive-associated venous thromboembolism: A systematic review and meta-analysis
Risk factors for antibody formation in children with hemophilia
Cardiovascular risk factors among adult patients with haemophilia
High risk of venous thromboembolism after orthopedic surgery in patients with thrombophilia
Risk of recurrent venous thromboembolism related to prior risk situations
Development of inhibitors in hemophilia A: an illustrated review
Mortality of patients with haemophilia in Brazil: First report
Role of Routine Laboratory Tests in Assessing Risk of Recurrent Venous Thrombosis: Results from the MEGA Follow-Up Study
Immune status of patients with haemophilia A before exposure to factor VIII: first results from the HEMFIL study
Hematologic variables and venous thrombosis: red cell distribution width and blood monocyte count are associated with an increased risk
Red cell distribution width and blood monocytes are associated with an increased risk of venous thrombosis
Risk of recurrent venous thrombosis related to past provoking risk situations: follow-up of a cohort study
The risk of venous thrombosis varies in different ethnic groups
The influence of prothrombotic laboratory abnormalities on the risk of recurrent venous thrombosis
The Risk of Venous Thrombosis in Different Immigrant Groups in the Netherlands
The Risk of Venous Thrombosis in Different Immigrant Groups in the Netherlands
Epidemiology of recurrent venous thrombosis
Past provoking venous thrombosis risk situations on the risk of a recurrent thrombotic event: A cohort study
The long-term course of factor VIII inhibitors in patients with congenital haemophilia A without immune tolerance induction